Fat cells symptoms and conditions

I can relate to many of these experiences. Started out in my 20's with very irregular cycles, went to my first gyn after a miscarriage - the emergency room dr referred me to a dr that was at a fertility clinic. I had no idea why until I was actual a little more "awake" I was diagnosed with polycystic ovaries. I went through at least 6 or 7 different birth control pills, depo provera shot, nuvaring, then back on another birth control pill. finally we started doing the continuous suppression as I was bleeding at least a little bit every single day... for 2 years. I would still have my full blown period every 4 weeks or so, which also included a monster migraine on day one of the menstruation. Not only was my life being altered but I was starting to get anemic. Finally after a month of the continuous suppression my bleeding stopped. As did the menstrual migraines. I continued this way for 4 years. Didn't have a single period or migraine, life was wonderful.. or so it seemed. I have been over weight for most of my adult life. Finally decided to do something about it. I joined the gym with a friend and started losing weight. I dropped 55 pounds until... the dreaded bleeding, pain and hormones got out of control. I started bleeding every single day again. Finally made an appointment with my dr. She stated that when you lose weight it releases estrogen out of your fat cells. Gee, I thought losing weight was supposed to make you feel better!! I went on with it for a while thinking it would stop eventually and it just HAD to get better. In fact, things got worse. I started having horrible abdominal pain, eventually it got to be daily. To the point where I could not stretch or even hyper extend my right leg backwards. My abdomen felt like something had a rubber band tied to it from the inside. My dr said that she suspected endometriosis. However, due to my anemia... we had to wait. So back on the iron pills and wait wait wait. Finally, October 15th I went in for my lap. Sure enough, stage 4 endo, huge cysts on both ovaries. My endo had gone all over the place and attached itself to anything it could. Including folding my bladder in half! Good grief. I thought that I was just getting the weak bladder from getting older (I am 35 by the way). For the next couple of weeks after my surgery I felt pretty good. Finally pain free (still a little bleeding but not much). But, the end of December rolls around and here it is, back with all its fury. The pain is again horrible, my migraines are back, my energy is dwindling. The good life was short lived. My doctor suggested a series of Lupron shots. One shot a month for 6 months. My first shot in January (took me a little bit of time to decide if I wanted to do it) finally bit the bullet and got the shot. First few days, fine, no problem, no relief either but no life altering experience. Then one morning I woke up and realized I was not in pain. It was a strange feeling actually. But the time I got the second shot, no more bleeding, no more pain... However, the hot flashes, night sweats and the emotions came on. Holy cow. Drama drama drama. I could find any reason on the planet to argue, with anyone. Thank god I have a very understanding family and an even more wonderful partner. I think he has the patience of a saint. I still don't know how he puts up with me. If I am not trying to find some reason to pick a fight then I am crying like a baby... for hours and hours. These hormones are so out of control. I honestly don't know what is worse, the pain or feeling like the world is going to end in the next 2 minutes if I don't get this spill picked up.. I literally cried for 2 hours Saturday because my cat knocked a stupid bottle of car wax off a shelf in the back room. Good lord, I had the most horrible feelings coming over me and just could not stop crying. I bought a new bed 2 weeks ago and let me tell you. If I am not on one of my 13 hour sleep fests then I am laying in it crying and feeling sorry for myself. Or the even better part of indegestion or my favorite part.. gas. I honestly don't know if I can go on like this. I made an appointment to see my doctorr this Friday to determine what she thinks will happen if I don't complete the other 3 shots. just give me back the pain if you have to!

I had a kenalog injection to my right cheek to treat a cyst. It ended up dilating the blood vessels and it atrophied the fat cells under the skin's surface. Now I have a permanent indent in my cheek that looks terrible. There is no way to cover it up and people ask about it all the time. It is very upsetting and stressful. I went to a different dermatologist and was told the only thing to do is a filler injection that only lasts up to 6 months at a cost of $525

I have taken lisinopril for more than 4 years and 2 days ago my tongue started swelling. It was about 9:00 p.m. and we were getting ready to go to bed when I realized it was getting worse. My tongue filled my mouth and protruded out and I couldn't swallow and could only speak with garbled words. My husband took me to the emergency room where they very quickly diagnosed it as an allergic reaction to lisinopril. I ended up in intensive care for the night. This was a very frightening experience, as well as terribly uncomfortable (and expensive). I spoke to my pharmacist today and he takes lisinopril. I told him to do some research and check out alternatives. I'd be interested to know the percentage of people who have similar, severe reactions to this drug.

I have been on Zyrtec for three years (Every day) haven't noticed mood swings in myself? My mother also takes them every other day and is not particularly moody. Although she has trouble sleeping which she attributes to the menopause But if i don't take one within 24hrs I get very itchy and hive up..now that I'm breastfeeding I've just noticed my daughter is very irritable..and am beginning to think it's related to the zyrtec. I'm changing to claratyne in the morning to see if there's a change..very,very interesting and scary reading all the side-effects!!

I thought I had Lupus because I had complete body aches for weeks. My bicep muscle in my right arm would feel like it was locked. I would wake up every morning feeling like I was in a car accident the day before. Once the body aches went away, I got blurred vision, burning in my eyes, headaches, fatigue, depression, problems concentrating... I just got this shot in June. I hope it metabolizes quickly and leaves my system w/o further side effects. I hope the indentation at the injection site fades away in time but I think it's permanent because the tissue has dissolved and the fat cells were destroyed. I wouldn't feel so bad if the indent wasn't in my face!

Cipro is a chemotherapeutic agent that is stored in fat cells and is reabsorbed into the bloodstream when burned and can potentially damage any system it comes in contact with. I took this for two weeks.and had horrible pains and kept having what could best be described as partial seizures and heart palpitations as well as peripheral neuropathies. As the drug recycles every few months back into my blood the symptoms start over and sometimes new ones occur. I am currently experiencing floaters, brain fog, vision problems, burning sensations, panic attacks, partial seizures, dizziness, depersonalization and extreme fatigue even nine months after taking 27 pills over the course of two weeks. Cipro is used to kill anthrax and should not be used on people even though Bayer is making a killing in its sales. You don't have to look far to find thousands of people who have had their lives destroyed by this drug. Remove from the market ASAP.

A silver-dollar sized indentation at the injection site (which was my left butt cheek) where it killed the fat cells in that one specific area